Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T28855 |
SSR126768A
SSR-126768A,SSR 126768A |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
SSR126768A 是一种新型且具有选择性、口服活性和有效性的催产素(OT)受体拮抗剂,对子宫收缩有抑制作用,可用于预防早产。 | |||
T28856 |
SSR180711 hydrochloride
SSR-180711A HCl,SSR-180711C HCl,SR-180711 HCl |
AChR | Neuroscience |
SSR180711 hydrochloride (SSR-180711A HCl) 是一种具有选择性的 Alpha7 尼古丁乙酰胆碱部分激动剂,可用于研究神经分裂和认知障碍。 | |||
T6082 |
SSR128129E
SSR |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SSR128129E (SSR) 是一种变构和口服活性 FGFR1 抑制剂 (IC50:1.9 μM),但不影响其他相关的 RTK。 | |||
T31095 |
Crinecerfont
SSR125543,SSR 125543,SSR-125543,SSR125543A,SSR 125543A,SSR-125543A |
CRFR | GPCR/G Protein |
Crinecerfont (SSR-125543) 是促肾上腺皮质激素释放因子 1 受体 (CRF1) 的特异性拮抗剂,可用于经典先天性肾上腺增生的研究。 | |||
T69140 |
Burapitant
SSR 240600 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Burapitant(SSR 240600)是一种新型非肽速激肽神经激肽 1 (NK) 受体拮抗剂,具有抗焦炉和抗抑郁活性。 | |||
T84293 |
SSR 180
|
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T5048 |
SSR240612
|
Bradykinin Receptor | GPCR/G Protein |
SSR240612 是口服有活性的非肽类缓激肽 B1 (bradykinin B1) 受体特异性拮抗剂。 | |||
T28857 |
SSR-182289A (Free)
SSR182289,SSR-182289A,SSR-182289,SSR 182289A,SSR182289A,SSR 182289 |
||
SSR-182289A (Free) is a thrombin inhibitor. | |||
T21989 |
SSR 69071
|
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SSR69071 是一种有效的,具有口服活性的选择性中性粒细胞弹性蛋白酶 (neutrophil elastase) 抑制剂。SSR69071 对人弹性蛋白酶 (Ki=0.0168 nM) 的亲和力高于对大鼠 (Ki=3 nM)、小鼠 (Ki=1.8 nM) 和兔 (Ki=58 nM) 弹性蛋白酶。SSR69071 减少缺血再灌注损伤后的心肌梗死面积。SSR69071 还具有治疗慢性阻塞性肺病、哮喘、肺气肿、囊性纤维化和多种炎症性疾病的潜力。 | |||
T13002 |
SSR-241586
|
Others | Others |
SSR-241586 is a neurokinin receptors antagonist,and is shown to be active in the treatment of depression, schizophrenia, urinary trouble, emesis, and irritable bowel syndrome (IBS). | |||
T23395 |
SSR 146977 hydrochloride
|
Others | Others |
NK3 receptor antagonist | |||
T28858 |
SSR504734
SSR-504734,SSR 504734 |
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SSR504734 is a novel potent glycine transporter 1 (GlyT1) inhibitor. | |||
T40775 |
SSR411298
SSR411298 |
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SSR411298 is a reversible, orally active compound that selectively inhibits fatty acid amide hydrolase (FAAH). Its potential lies in the field of post-traumatic stress disorder (PTSD) research. | |||
T40398 |
Crinecerfont hydrochloride
SSR-125543A,SSR-125543 hydrochloride |
||
Crinecerfont hydrochloride (SSR-125543) is a highly potent, orally active, non-peptide antagonist of the CRF1 receptor. It has demonstrated efficacy in the context of Classic congenital adrenal hyperplasia (CAH) research. | |||
T13003 |
SSR128129E free acid
SSR free acid |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SSR128129E free acid is an orally available and allosteric inhibitor of FGFR(IC50 of 1.9 μM for FGFR1). | |||
T15276 |
Ferroquine
SSR97193,Ferrochloroquine |
Others | Others |
Ferroquine (Ferrochloroquine) 是 Chloroquine 的二茂铁基类似物,具有抗疟疾活性。Ferroquine 具有杀疟原虫作用,机制是通过诱导氧化应激和随后的膜破坏。 | |||
T90597 |
SSR504734 HCl
|
||
SSR504734 是一种具有口服活性、选择性和可逆性的 GlyT1抑制剂 (hGlyT1,rGlyT1,mGlyT1IC50分别为 18、15 和 38 nM)。SSR504734 在精神分裂症、焦虑症和抑郁症模型中表现出活性。 | |||
T28153 |
Nelivaptan
SSR149415,SR 149415,SR-149415 |
Vasopressin Receptor | GPCR/G Protein |
Nelivaptan (SR 149415) 是一种加压素 V1b 受体拮抗剂。 | |||
T11006 |
Desmethyl ferroquine
SSR97213 |
Others | Others |
Desmethyl ferroquine is the active and major metabolite of Ferroquine.Desmethyl ferroquine shows significant activity against Chloroquine-susceptible and resistant P. falciparum strains. Ferroquine is an antimalarial. | |||
T60126 |
4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1A)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine
|
Others; CRFR | GPCR/G Protein; Others |
4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1A)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine 是SSR-125543的对映异构体. SSR-125543是一种有效的CRF-R1拮抗剂,对人CRF-R1的Ki=1.0nM。 |